TW314528B - - Google Patents
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- TW314528B TW314528B TW082109695A TW82109695A TW314528B TW 314528 B TW314528 B TW 314528B TW 082109695 A TW082109695 A TW 082109695A TW 82109695 A TW82109695 A TW 82109695A TW 314528 B TW314528 B TW 314528B
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- Taiwan
- Prior art keywords
- group
- alkyl
- formula
- hydrogen
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- -1 tetramethylpiperidinyl Chemical group 0.000 claims abstract description 43
- 229920001577 copolymer Polymers 0.000 claims abstract description 33
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 24
- 239000000203 mixture Substances 0.000 claims abstract description 20
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 17
- 239000004711 α-olefin Substances 0.000 claims abstract description 14
- 239000003381 stabilizer Substances 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 10
- 239000001257 hydrogen Substances 0.000 claims abstract description 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 5
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims abstract description 3
- 150000002431 hydrogen Chemical class 0.000 claims abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 10
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- YAXWOADCWUUUNX-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidine Chemical group CC1CCCN(C)C1(C)C YAXWOADCWUUUNX-UHFFFAOYSA-N 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 claims description 4
- 229910000071 diazene Inorganic materials 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 150000001993 dienes Chemical class 0.000 claims description 3
- 150000002466 imines Chemical class 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- JOBALMNTXJSMJJ-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidin-4-amine Chemical compound CC1C(N)CCN(C)C1(C)C JOBALMNTXJSMJJ-UHFFFAOYSA-N 0.000 claims description 2
- YTPCNCOVEFRSOV-UHFFFAOYSA-N 5-iminopyrrol-2-amine Chemical compound N=C1NC(=N)C=C1 YTPCNCOVEFRSOV-UHFFFAOYSA-N 0.000 claims description 2
- 229910014585 C2-Ce Inorganic materials 0.000 claims description 2
- 150000003973 alkyl amines Chemical class 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 230000005611 electricity Effects 0.000 claims 1
- 239000000779 smoke Substances 0.000 claims 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 abstract description 8
- 239000011368 organic material Substances 0.000 abstract description 8
- 239000003973 paint Substances 0.000 abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 2
- 125000003944 tolyl group Chemical group 0.000 abstract description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 239000011814 protection agent Substances 0.000 abstract 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 11
- 229920003023 plastic Polymers 0.000 description 11
- 239000004033 plastic Substances 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 11
- 238000000576 coating method Methods 0.000 description 10
- 239000005977 Ethylene Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 6
- 238000011049 filling Methods 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 5
- 239000004611 light stabiliser Substances 0.000 description 5
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 3
- YCOZIPAWZNQLMR-UHFFFAOYSA-N heptane - octane Natural products CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- CRSOQBOWXPBRES-UHFFFAOYSA-N neopentane Chemical compound CC(C)(C)C CRSOQBOWXPBRES-UHFFFAOYSA-N 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- BSSNZUFKXJJCBG-UPHRSURJSA-N (z)-but-2-enediamide Chemical compound NC(=O)\C=C/C(N)=O BSSNZUFKXJJCBG-UPHRSURJSA-N 0.000 description 2
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- PTXRXGQLWLINGT-UHFFFAOYSA-N cyanic acid;urea Chemical compound OC#N.NC(N)=O PTXRXGQLWLINGT-UHFFFAOYSA-N 0.000 description 2
- 125000006159 dianhydride group Chemical group 0.000 description 2
- QWHNJUXXYKPLQM-UHFFFAOYSA-N dimethyl cyclopentane Natural products CC1(C)CCCC1 QWHNJUXXYKPLQM-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- NDJKXXJCMXVBJW-UHFFFAOYSA-N heptadecane Chemical compound CCCCCCCCCCCCCCCCC NDJKXXJCMXVBJW-UHFFFAOYSA-N 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- HGEMCUOAMCILCP-UHFFFAOYSA-N isotridecane Natural products CCCCCCCCCCC(C)C HGEMCUOAMCILCP-UHFFFAOYSA-N 0.000 description 2
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 1
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1 -dodecene Natural products CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 1
- FFIJIFGRYNWQNQ-UHFFFAOYSA-N 1-(2,2,6,6-tetramethylpiperidin-4-yl)pyrrole-2,5-dione Chemical compound C1C(C)(C)NC(C)(C)CC1N1C(=O)C=CC1=O FFIJIFGRYNWQNQ-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 1
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 1
- JTIHSSVKTWPPHI-UHFFFAOYSA-N 2-amino-2-phenylacetonitrile Chemical class N#CC(N)C1=CC=CC=C1 JTIHSSVKTWPPHI-UHFFFAOYSA-N 0.000 description 1
- TVONJMOVBKMLOM-UHFFFAOYSA-N 2-methylidenebutanenitrile Chemical compound CCC(=C)C#N TVONJMOVBKMLOM-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- RQWDXNAIEYQSPX-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)(=O)O.C(CCCCCCCCCCCCCCCCC)(=O)O.OP(O)OP(O)O.OCC(CO)(CO)CO Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)O.C(CCCCCCCCCCCCCCCCC)(=O)O.OP(O)OP(O)O.OCC(CO)(CO)CO RQWDXNAIEYQSPX-UHFFFAOYSA-N 0.000 description 1
- FUPBAJNBVNGHGH-UHFFFAOYSA-N CCCCCCCCCCCCCCCCCC.CCCCCCCCCCCCCCCCCC.S(CCC(=O)O)CCC(=O)O Chemical compound CCCCCCCCCCCCCCCCCC.CCCCCCCCCCCCCCCCCC.S(CCC(=O)O)CCC(=O)O FUPBAJNBVNGHGH-UHFFFAOYSA-N 0.000 description 1
- 239000004716 Ethylene/acrylic acid copolymer Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- GFSXGLIQRNJCOC-UHFFFAOYSA-N P(O)(O)O.P(O)(O)O.C1(=CC=CC=C1)C1=CC=CC=C1 Chemical compound P(O)(O)O.P(O)(O)O.C1(=CC=CC=C1)C1=CC=CC=C1 GFSXGLIQRNJCOC-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GQSQSXNXGJOTLZ-UHFFFAOYSA-N S(CCC(=O)O)CCC(=O)O.CCCCCCCCCCCC.CCCCCCCCCCCC Chemical compound S(CCC(=O)O)CCC(=O)O.CCCCCCCCCCCC.CCCCCCCCCCCC GQSQSXNXGJOTLZ-UHFFFAOYSA-N 0.000 description 1
- NAMKRUKTHCTWGN-UHFFFAOYSA-N S(CCC(=O)O)CCC(=O)O.CCCCCCCCCCCCCC.CCCCCCCCCCCCCC Chemical compound S(CCC(=O)O)CCC(=O)O.CCCCCCCCCCCCCC.CCCCCCCCCCCCCC NAMKRUKTHCTWGN-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000007860 aryl ester derivatives Chemical class 0.000 description 1
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- MSZJEPVVQWJCIF-UHFFFAOYSA-N butylazanide Chemical compound CCCC[NH-] MSZJEPVVQWJCIF-UHFFFAOYSA-N 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000005465 channeling Effects 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001887 cyclopentyloxy group Chemical group C1(CCCC1)O* 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000006286 dichlorobenzyl group Chemical group 0.000 description 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical group CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical compound C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 description 1
- CEIPQQODRKXDSB-UHFFFAOYSA-N ethyl 3-(6-hydroxynaphthalen-2-yl)-1H-indazole-5-carboximidate dihydrochloride Chemical compound Cl.Cl.C1=C(O)C=CC2=CC(C3=NNC4=CC=C(C=C43)C(=N)OCC)=CC=C21 CEIPQQODRKXDSB-UHFFFAOYSA-N 0.000 description 1
- 125000005909 ethyl alcohol group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- SHCBAMFXPADYCS-UHFFFAOYSA-N hexanedioic acid;piperidine Chemical class C1CCNCC1.OC(=O)CCCCC(O)=O SHCBAMFXPADYCS-UHFFFAOYSA-N 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000006115 industrial coating Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- WFKAJVHLWXSISD-UHFFFAOYSA-N isobutyramide Chemical compound CC(C)C(N)=O WFKAJVHLWXSISD-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000006178 methyl benzyl group Chemical group 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- IAHOMKOOEHIHGD-UHFFFAOYSA-N octadecyl acetate propanoic acid Chemical compound C(CC)(=O)O.C(C)(=O)OCCCCCCCCCCCCCCCCCC IAHOMKOOEHIHGD-UHFFFAOYSA-N 0.000 description 1
- 150000003891 oxalate salts Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000007539 photo-oxidation reaction Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 229920000962 poly(amidoamine) Polymers 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920001652 poly(etherketoneketone) Polymers 0.000 description 1
- 229920000333 poly(propyleneimine) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 229910052705 radium Inorganic materials 0.000 description 1
- HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical group [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/36—Amides or imides
- C08F222/40—Imides, e.g. cyclic imides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/14—Monomers containing five or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Description
314528 Α6 Β6 五、發明説明(1 ) 本發明係關新穎順丁烯二醯亞胺/ α-烯烴共聚物*其製 法·其作光安定劑及有機物質的安定劑之用途*特別供塑 膠與塗料用,及用此等共聚物安定之有機物質。 咸知有機物質尤其塑膠與塗料極快破壞,特別為光作用 之結果。此棰毀壞通常顯現變黃 > 褪色,或材料破裂或脆 化。因此意欲Κ光安定劑及安定劑供應滿意的保護予有機 材料對抗光、氧及熱的毀損。 舉例DE-C 30 24 525 ( 1 )敘述陽離子型順丁烯二酐聚合 物含i)-90莫耳%之未取代的或取代的乙烯單位與10-1 〇〇莫 耳!《之順丁烯二酐單位,其中高達67-95!^與4-胺基-2,2, 6,6 -四甲基哌啶轉化成亞胺。此等聚合物適供塑膠對光化 學及熱分解安定化。可用的取代乙烯單位包括諸有 Ci-Cw烷基圑者,即適宜的相當單體姐分為C3-C22-ot 烯烴類。所述共聚物含順丁烯二酐單位與乙烯單位宜成1 :1比,較佳有分子最自1,〇〇〇至2,000,000 。 GB-A 2 145 100 (2)敘述一種N -多烷基哌啶基取代的順 丁烯二醸亞胺例N-(2,2,6,6 -四甲基-4-哌啶基)順丁烯二 醢亞胺與(:3~(:2<>-£*-烯烴之共聚物。此共聚物適作塑膠用 光安定劑。α -烯烴之例為卜十二碳烯及1-十八碳烯。所 述共聚物有平均分子量自1,000至50,000,較佳1,000至 5,000 〇 (諳先閲讀背面之注意事項再填寫本頁) .裝. 、1Τ, 經濟邹中央標準局貝工消費合作社印製 DD-A 262 439 (3)敘述一種使聚合物對光與氧化作用安 定化的方法,用三聚物、多聚物或接枝聚合物Μ含多烷基 哌啶的順丁烯二酸衍生物如Ν-(2,2,6,6-四甲基-4-哌啶基
衣紙張尺度適用中國國家標準(CNS)甲4規格(210 X 29?公釐) 五、發明説明( )順丁烯二醯 位如 C3-C20·· c 酐、順丁烯二 三姐分之化合 M-上取代。所 較佳自800至 在此等Μ往 時期保護作用 及熱分解作用 本發明之一 材料之安全劑 吾人已發現 二醯亞胺/ α - A6 B6 亞胺作第一組分,未取代的或取代的乙烯單 ί烯烴作第二姐分及順丁烯二酸、順丁烯二 醯胺或順丁烯二醸亞胺作第三姐分,其中第 物可進一步為烷基、芳烷基或苯基於0-或 述聚合物有自800至150,000之相對分子虽, 12,000 ° 技術用劑之情況中與塑膠之不良相容性、短 、物質之天然色、升溫摻併時安定劑揮發性 之趨勢仍經常不圓滿。" 目的在提供光安定劑與保證更有效保護有物 0 此目的可用如下式I結構單位”姐成的順丁烯 烯烴共聚物達到
CH2 —CH- I R2 其中R1為式I之四甲基哌啶基團
CHj CH3 (請先閱讀背面之注意事項再填寫本頁) '裝, '1T. (I)
(ID 严 經濟部中央標準局員工消費合作社印製 R 3係氫、C ^ - C β烷基、甲醯基、c 2 - C β烷醢基、C 1 - C12烷氧 基、Cs或Ce瓌烷氧基、氰甲基、2-羥乙基、苄基或 4- 本紙張尺度適用中國國家標準(CNS)甲4规格(210 X 297公赞) 經濟部中央標準局員工消f合作社印製 A6 _B6_ 五、發明説明(了 ) -CR4 = CH-C0-0Rs式之基團’ R4為氫、Ci-Ce综基或一 _CO-ORB式基團’及 {^係〇1-〇18烧基、Cs-Ca環燒基、C7_Cia芳燒基、本基或 苯甲基*及 KI為基礎多達8莫耳S!之卩1可再係氫、Ci-Cu烷基或 CB-Ce瓖烷基,及 R2為C14-C28烷基之混合物’其中二個此等烷基可相差不 超遇二個碳原子者各佔此混合物之至少30¾ ,有平均分子 量自 1,000至 50,000。 順丁烯二醸亞胺/ α -烯烴共聚物有自1,500至10,000, 特別自2,000至5,000之平均分子量者較佳。所述分子最為 數均分子量。 R2為Cl4-Cza院基、較佳Cie_Cz4焼基、特別Cia_C22燒 基等之混合物,即共聚物係基於Cie-C3〇- (X -烯烴類、較 佳Cia-C2e- CX -烯烴、特別C2Q-CZ4- α烯烴等作合成嵌段 。R2宜係直链烷基。 須知烷基混合物作Rz之存在意謂作為含全部共聚物總數 間之統計平均、相差不超過2碳原子之二特殊烷基各佔此 混合物之至少30 % ,較佳至少40 % 。此等特別為三涸特殊 烷基例為十八碳烷、廿碳烷及廿二碳烷基之混合物,其中 此等相差2碳原子之二個基佔混合物之40¾ Μ上,第三基 佔3至18¾ ;混合物內可含少量略低於18或稍多於22碳原 子的其他烷基,其量常在2¾以下。 適宜R3與PiCa-Ce烷基團、基團及Ri之 Ci -C22烷基團為分枝的及特別直鏈的基團,尤其甲,乙、 -5- 本紙張尺度適用+ a ®家樓準(G刷甲视格(210x 297公愛) "~'' - f 、...................f..........Γ!.........._、............ .................裝......................訂.....................線 (請先閲讀背面之注意事項再填寫本頁〕 經濟部中央標準局員工消費合作社印製 A6 ____ B6_______ 五、發明説明(4 ) 正丙、異丙、正丁、異丁、另丁、特丁、正戊、異戊、另 戊、特戊、新戊、正己、正庚、正辛、2-乙基己、正壬、 異壬、正癸、正十一烷、正十二烷、正十三烷、異十三烷 、正十四烷、正十五烷、正十六烷、正十七烷、正十八烷 、正十九烷、正廿烷及正廿二烷等基。 適宜直鐽或支鍵的C2-Ce烷醯基團R3特別為乙釀、Μ及 丙醢、丁醯、異丁醯、戊酿及己釀等基團,。 特別適宜的直鐽或分枝的烷氧棊R3gCe-C8烷氧 基諸為正己氧、異己氧、正辛氧、2-.乙棊己氧及異辛氧, 以及甲氧、乙氧、正丙氧、異丙氧、正丁氧、異丁氧、另 丁氧、特丁氧、正戊氧、正壬氧、正癸氧、正十一烷氧及 正十二烷氧等基。 R3之Cs-與Ce-環烷氧基特別為環戊氧與環己氧等基。 特別適當C5-Ca環烷基團R1及Rs為環戊與環己以及環庚 、環辛、甲基環戊、二甲基環戊、甲基環己、乙基環己及 二甲基環己等基围。 «宜C7~Cla芳烷基團1^之例為萘甲、二苯基甲及甲基节 等基團’但特別為Ct-Cis或燒基諸為1-苯乙、2 -苯乙、 1_苯丙、2 -苯丙、3_苯丙、2_苯丙~2-基、4 -苯丁、2, 2-二甲基-2-苯乙、5-苯戊、10-苯癸、12-苯基十二焼等 基團,尤其苄基。 適宜甲苯基圏為鄰-、間-及特殊對甲苯基。 R1宜係四甲基哌啶基團]1,其中R3為氲、Cl_Ce综基特 別甲基、或一 - CH = CH-C0-0ReS之基團,其中RegCi_Ce -6 * 本紙張尺度適用中國國家標準.(CNS)甲4规格(210 X 297公釐) (請先閲讀背面之注意事項再填寫衣頁) f 丨裝. 訂· 314528 Afi A6 B6 五、發明説明(5 烷基,特別為_甲基或乙基。 須知Μ II為基準在順丁烯二醢亞胺的氮上存在多逹8 、 特別最多5莫耳%之氫、C:l-C22烷基或CB-Ca環烷基作取 代基R1意謂此四甲基哌啶基團I與其他取代基I之混合物 能在與結構單位I存在的全部共聚物分子之總數間出現為 铳計的平均。摻併少量與四甲基哌啶取代基不同的基團 R1結果產生稍微修改的新穎順丁烯二醢亞胺/ « -烯烴共聚 物之性質。 本發明因此敘述種製備新穎順丁烯二醯亞胺/ α -烯烴 共聚物之方法,其中一項由式I結構單位姐成的順丁烯二 酐/ α -烯烴共聚物
CH2—CM- i R2 (請先閲讀背面之注意事項再填寫衣頁) (III) 與通式IV之4-胺基四甲基哌啶 NH,
N i R3 h3c h3c ch3 (IV) 經濟部中央標準局員工消費合作社印製 及如須要時MIV為基準多達8 、特別最多5箅耳S:之氨’ —Ci-Cu烷胺或Ce-Cs環烷肢在有機溶劑内於1〇〇至220¾ 反應。I內酐基對伯胺IV之克分子比有利地為1 :1或大約 7- 本紙張尺度適用中國國家標準(CNS)甲4规格(210 X 297公釐) 經濟部中决標準局員工消費合作社印製 A6 _. _'_B6___ 五、發明説明(6 ) 1:1° 特別合宜的有機溶劑為芳鼷烴類如甲笨、二甲苯或三甲 基笨,及鹵烴類或硝基烴類如氯苯、二氯笨或硝基苯。此 等芳鼷化合物之工業混合物特別重要。但如非芳麇烴混合 物有適當高沸點則亦可用。 反應溫度應較佳選擇自120至200Ϊ:,特別自140至175C 。反應生成的水有利地餾出共沸混合物。反應通常於大鮮 壓力進行,一般於1至5小時後完全。 具結構單位I且作始材料用的順丁烯二酐/ α-烯烴共聚 物能用已知製法獲得,由順丁烯二酐與相當 α-烯烴混合 物之聚合作用,例如類似Houben-Weyl,有機化學方法( 德文),E20/2 卷,第 1237-1248 頁(1987)。 有结構單位I的新穎顒丁烯二醢亞胺/ 〇c-烯烴共聚物及 有结構單位ϋ並用作始材料之順丁烯二酐/ α-烯烴共聚物 二者一般均係順丁烯二酸衍生物與烯烴的交替單位姐成之 1 : 1共聚物。 新穎順丁烯二醢亞胺/ α -烯烴共聚物極有效安定有機材 料對光、氧及熱之作用。此等於有機材料製備之前或後或 製備期間Κ有機材料重量基自〇.〇1至5 ,較佳自0.02至 IX之澹度加進待安定化的有機材料内。 須知有機材料係指例如化敉製品如軟資與洗灌劑,葯物 方劑如葯丸及栓劑等,攝影記錄材料如顯像乳液等或塑膠 及塗料之中間物,但特別為塑膠與塗料本身。 本發明又闞有機物質特別為塱膠或塗料經安定化Κ抗光 (請先閱讀背面之注意事項再塡寫本買) f 裝. 訂. Μ -8 - 本紙張尺度適用中國國家標準(CNS)甲4规格(2〗0 X 297公釐) 經濟部中央標準局員工消費合作社印製 A6 _______B6 __ 五、發明説明(7 ) 、氧及热之作用,並含前述濃度之新穎共聚物。 所有已知混合安定劑或其他添加劑於聚合物內之裝置及 方法皆可用以混合新穎共聚物特別與塑膠。 經新頴共聚物安定化的有機物質亦可含另外添加劑例如 抗氧劑、光安定劑、金靥減活化劑、抗靜窜劑、難燃劑、 顔料及填料等。 新穎共聚物K外可另加進之抗氧劑及光安定劑為例如K 空間位阻的酚類之化合物或含硫或磷的輔安定劑。 此等酚型抗氧劑之實例為2,6-二特丁-4-甲基苯酚,冷 -(3,5-二特丁-4-羥笨基)丙酸正十八烷醋,1,1,3-三 (2-甲-4-羥-5-特丁基笨基)丁烷,1,3,5-三甲-2,4,6-三 -(3,5-二特丁 -4-羥苄基)笨,1,3,5-三-(3,5-二特丁 -4-羥苄基)、異尿氰酸酯,1,3,5-三-〔/8-(3,5-二特丁 -4-羥苯基)-丙醸乙基〕異尿氰酸酯,1,3,5-三-(2,6-二 甲-3-羥-4-特丁基苄基)異尿氰酸酯及四-〔卢-(3,5-二 特丁 -4-羥笨基)丙酸〕季戊四醇酯。 適用含磷抗氧劑之實例為亞磷酸三(壬基苯)酯,季戊 四醇二亞磷酸二硬脂酸醅,亞磷酸三(2,4-二特丁基笨)_ ,亞磷酸三(2-特丁 - 4-甲基苯)酯,二亞磷酸雙(2, 4-二特 丁基笨基)季戊四酵酯與四- (2,4-二特丁基笨基)4,4’-、 伸聯苯二亞磷酸酯。 含硫抗氧劑之例為硫代二丙酸二(十二烷)酯,硫代二丙 酸二(十四烷)酿,硫代二丙酸二(十八烷)酯,四-(於-十 二烷基硫代丙酸)季戊四醇幽與四-(召-己基硫代丙酸)季 (請先閲讀背面之注意事项再填寫衣頁) 本紙張尺度適用中國國家標準(CNS)甲4规格(210 X 297幺釐) A6 B6 經濟部中央標準局員工消费合作社印製 五、發明説明(8 ) 戊四醇酿。 可與新穎共聚物一起使 為2-(2’-羥苯)基苯并三 甲酸類之芳酯,α-氰基 笨胺,鎳化合物或草醢替 可用新穎共聚物安定化 合物如低密度與高密度聚 ,聚異戊間二烯及聚丁二 所述聚合物之混合物;單 共聚物例如乙烯/丙烯酸 酯共聚物,乙烯/醋酸乙 物;聚苯乙烯及苯乙烯及 烯醯衍生物之共聚物例如 (SAN),苯乙烯/異丁烯酸 酯,苯乙烯/丙烯腈異丁 (ABS)或異丁烯酸甲酯/丁 例如聚氯乙烯,聚氟乙烯 由α,/9-不飽和酸類及其 酯,聚異丁烯酸酯,聚丙 與胺或自其丙烯醢衍生物 乙烯酵及聚醋蟫乙烯酯; 聚酯、聚碳酸_、聚飆、 新穎共聚物亦能用以安 中值得特別注意者為烤漆 用的其他抗氧劑及光安全劑舉例 唑,2-(羥基)二苯甲酮,羥基笨 肉桂酸衍生物,笨并味唑羰釀替 二苯胺。 的塑膠實例為:單-及雙烯烴之聚 乙烯,聚丙烯,線型聚丁 -1-烯 烯,與單-或雙-烯烴之共聚物或 -或雙-烯烴與其他乙烯基單體之 烷酯共聚物,乙烯/異丁烯酸烷 烯酯共聚物或乙烯/丙烯酸共聚 ct-甲基苯乙烯與二烯類及/或丙 笨乙烯/ 丁二烯,苯乙烯/丙烯腈 乙酯,苯乙烯/丁二烯/丙烯酸乙 烯酸酯,丙烯腈/ 丁二烯/苯乙烯 二烯/苯乙烯(MBS);含鹵聚合物 ,聚偏二氟乙烯及其共聚物等; 生物等衍生的聚合物如聚丙烯酸 烯醯胺及聚丙烯腈;由不飽和酵 或縮醛類等衍生的聚合物例如聚 聚胺基甲酸酯、聚醯胺、聚腺、 聚醚踽及聚醚酮。 定化塗料例如工業用塗料。此等 ,此中依序為車輔塗料,較佳二 -10 本紙張尺度適用中國國家標準(CNS)甲4规格(210 X 297公釐) 請 先 閱 讀 背 面£ 之 注 意 事- 項; 再 塡 'S 頁 裝 訂 Λ 經濟部中央標準局員工消費合作社印製 A6 B6 _ 五、發明説明(9 ) 餍塗料。亦可用K例如作建物外層、其他結構或工業裝置 之塗復材料。 新穎共聚物可用固體或溶解式加入塗料。其在塗料糸統 中的良好溶解度特別有利。 新穎共聚物較佳用Μ安定化聚醸胺及ABS與SAK聚合物, 尤其在含有此等之模塑材料及塗料上。 更佳使用領域為安定化低密度與高密度聚乙烯及聚丙烯 與聚醱胺,例如亦安定其所製造的纖維等。 由於其抗移動性、.新穎共聚物特別適合供安定有高比率 表面積對體積之物品特別如膜、帶及纖維等。 新穎共聚物展現與傅统型塑膠之良好相容性及在傅统塗 料系統中有良好溶解度與優越相容性。通常其等甚少或全 無自然色,在塑膠與塗料等一般加工溫度稱定,且不揮發 ,並特別供給經其處理過的材料長期保護。 顯著的結果在一新穎順丁二烯醢亞胺/ « -烯烴共聚物其 R2含Cia-C22烷基(見實例)之混合物者與(2)内掲示的相 彷順丁二醸亞胺/ «-烯烴共聚物比較於其作用方面有實質 的儍點,其中R2係Cle烷基(見比較實例A)經二共聚物在聚 丙烯射入模製的零件之明白交代的對比證明。 寊例 117g之4-胺基-2,2, 6, 6-四甲基哌啶於20分鐘期間逐滴加 入20 3g —項順丁烯二酐與下列成分的α -烯烴替換之1:1共 聚物混合物: 十八碳-1-烯 1%重董比 (請先閱讀背面之注意事項再塡寫本頁) 裝- '1Τ, -11*· 本紙張尺度適用中國國家標準(CNS)甲4規格(210 X 297公釐) 314528 A6 B6 五、發明説明(10: 廿碳-1-烯 廿二碳-1-烯 廿四碳-1-烯 廿六碳-卜烯 49¾重量比 42¾重量比 8!«重董比 < 0 .1重量比 經濟部中央標準局員工消費合作社印製 在40 0 ml之商品芳烴混合物内有沸點範圃160-170¾混合 物鼸後加熱至沸騰並再於同溫度歷180分鐘。當水雔器中 不再有水分出時減壓下餾脫溶劑。磨细固化的熔融物,得 250g之1(2,2,6,6-四甲基4-哌啶基)順丁烯二醢亞胺 •/C2〇-C24-cx-烯烴共聚物,呈淡黃色粉狀,熔點104-111 Ό 〇 比較實例A 自與實例相彷替換1:1順丁烯二酐/十八碳-卜烯共聚物 製備熔點60-69¾之N-(2,2,6,6-四甲基-4-哌啶基)順丁烯 二醸亞胺/十八碳-1-烯共聚物。 Μ效特猷 聚丙烯試驗標本之製法 溶解實例或比較實例Α中0.5%重量之安定劑於 }<<^〇1611@1100(:型的聚丙烯内係於熔化溫度24 010時一次擠 壓,於240¾將所得顆粒注射模塑而得2 m®厚之試驗標本。 試驗標本在Xenotest® 1 200加速耐候裝置中測試驗標本 的耐光性與耐候性。試驗標本之表面特徴作耐候時間的函 數係聚合物光氧化作用變質之衡量。因此記錄出現第一破 裂所經歷時間。 -1 2 - 本紙張又度通用中國國家標準(CNS)甲4规格(21.0 X 297公釐) (請先閱讀背面之注意事項再塡寫本頁) Λ __ I— n n • I I . ——tr—— S14528 Αβ ___Β6_ 五、發明説明(ϋ) 在其中含比較實例A中K往技術安定劑的試驗標本內僅 2,50 0小時後發生破裂,而在含實例中新穎安定劑的試驗 標本內並未出現破裂直到3,000小時後。 (請先間讀背面之注意事項再塡寫本頁) Λ 裝--- 訂-- 經濟部中央標準局員工消費合作社印製 -13- 本紙張尺度適用中國國家標準(CNS)甲4規格(210 X 297公釐〉
Claims (1)
- 314iir 中文申請專利範1修正本(年6月 M)5號專利申請案,Β修正一 年月曰 掷·β·之補充 申請專利範圍 一種由如下式I结構單位组成的頓丁烯二薩亞胺/ ct -烯 烴共聚物* ·— CH - 丫 \〇 I R1 R2 其中R1為式I之四甲基哌啶基團(I) (II) R3係氫、Ca-Ce烷基、甲藤基、C2-Ce烷藤基、(^-(:^烷 氧基、(:5或U環烷氧基、氰甲基、2-羥乙基、苄基或 -CR4 = CH-C(1-0R5式之基團, R"4為氫、烷基或化學式為- CO-OR5之基團,及 R 5澎C X - C ^ 8烷基、C s - C 8環烷基、C 7 - C a s芳烷基、笼基 或甲茏基,及 閱 1 讀 背* · I 面· | 之 I 注 拿··丨 項|翁叫 .寫Μ本, I I 訂 經濟部中央標準局員工消費合作社印製 Mcl Π ¾ 高 MC5 , 或 準基 基烷 為 2 2 C. 環 e C 氫 為 步 1 進 可 1 R 之之 及 耳 ’ 莫基 8 垸 .1 C 為超 2 K R 孑 過 S 差平 相有 可具 基, 烷 等 此少 個至 二之 中物 其合 ’混 物此 合佔 混各 之 , 基子 烷原 8碳 2 1 C 個 % ο 3 / 胺 亞 m 二 烯 丁 腊: 之 項 1—< 第 圍 範 利 - 專 05請 00.* 1,摈 自根 量辑 子製 分種 均 一 ο ο ο ο 5 本纸張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) I ^ ml Tmfl nn 8 254 J 8 8 88 ABCD 申請專利範圍 α -烯烴共聚物之方法,其中令式I结構單位组成的顆 丁烯二酐/ α -烯煙共聚物 _ Cfi'2 — CH- I 〇/ 〇’ \〇 R2 輿式Γ·/之4 -胺基四甲基哌啶 νή2ch3 gh3 (III) (IV) 閏讀,! 背,I 面=I 之 % -I I 1 I ί^ιί f 頁i 經濟部中央標準局員工消費合作社印製 i如有須要時蚁IV為基準多達s莫耳I之氨,一種 “-C2i;烷胺或Cs-“環烷胺在有樣溶劑中於100至220¾ 反應。 3. 根據申請專利範圍第1項所界定之順丁烯二裔亞胺/ α -烯烴共聚物,其用作光、氧及熱之安定劑,其中該顒 丁烯二藤亞胺/ α-烯烴共聚物所使兩之濃度為0.01至 5電量妬。 本紙張尺度逋用中國國家標準(CNS ) A4规格(210X297公釐)
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| DE4239437A DE4239437A1 (de) | 1992-11-24 | 1992-11-24 | Maleinsäureimid-alpha-Olefin-Copolymerisate und ihre Verwendung als Lichtschutzmittel und Stabilisatoren für organisches Material |
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| JP2009502852A (ja) * | 2005-07-25 | 2009-01-29 | ビーエーエスエフ ソシエタス・ヨーロピア | 皮膚化粧品調製物 |
| DE102005061954A1 (de) | 2005-12-23 | 2007-07-05 | Basf Ag | Verfahren zur Wiedergewinnung von Ruthenium aus gebrauchten Rutheniumoxid-haltigen Katalysatoren |
| JP5393157B2 (ja) | 2006-01-13 | 2014-01-22 | ビーエーエスエフ ソシエタス・ヨーロピア | 安定剤混合物 |
| DE502008002175D1 (de) | 2007-08-28 | 2011-02-10 | Basf Se | Stabilisatormischung |
| JP5602352B2 (ja) | 2007-09-21 | 2014-10-08 | 住友化学株式会社 | 光安定化ポリプロピレン |
| US8513361B2 (en) | 2007-12-28 | 2013-08-20 | Bridgestone Corporation | Interpolymers containing isobutylene and diene mer units |
| CN102137889B (zh) | 2008-08-28 | 2013-11-13 | 巴斯夫欧洲公司 | 用于无生命有机材料的稳定剂 |
| WO2010072768A1 (de) | 2008-12-23 | 2010-07-01 | Basf Se | Uv-absorber agglomerate |
| CN103168053B (zh) * | 2010-10-20 | 2015-11-25 | 巴斯夫欧洲公司 | 具有特定功能化的低聚光稳定剂 |
| JP2014196379A (ja) * | 2013-03-29 | 2014-10-16 | 住友化学株式会社 | ポリプロピレン樹脂組成物 |
| DE102014210214A1 (de) * | 2014-05-28 | 2015-12-03 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von Oxyimid-enthaltenden Copolymeren oder Polymeren als Flammschutzmittel, Stabilisatoren, Rheologiemodifikatoren für Kunststoffe, Initiatoren für Polymerisations- und Pfropfprozesse, Vernetzungs- oder Kopplungsmittel sowie solche Copolymere oder Polymere enthaltende Kunststoffformmassen |
| CN107573324A (zh) * | 2017-10-23 | 2018-01-12 | 山西省化工研究所(有限公司) | 一种聚合型受阻胺光稳定剂gw‑5050的制备方法 |
| CN108192003B (zh) * | 2017-12-29 | 2020-01-21 | 中山大学 | 一种自由基化乙烯马来酸酐共聚物及其合成方法 |
| CN108659233B (zh) * | 2018-06-19 | 2021-11-16 | 中红普林医疗用品股份有限公司 | 一种橡塑用自由基猝灭型高分子光稳定剂 |
| CN109517108B (zh) * | 2018-10-22 | 2021-04-02 | 乐凯化学材料有限公司 | 制备马来酰亚胺/α-烯烃共聚物的方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3024525A1 (de) * | 1980-06-28 | 1982-02-04 | Chemische Werke Hüls AG, 4370 Marl | Kationische maleinsaeureanhydrid-homo- und copolymerisate sowie deren verwendung |
| GB2145100A (en) * | 1981-08-12 | 1985-03-20 | Ciba Geigy Ag | Copolymeric polyalkylpiperidines |
| US4520171A (en) * | 1982-05-05 | 1985-05-28 | Hercules Incorporated | Polymeric hindered amines |
| US4866136A (en) * | 1987-08-12 | 1989-09-12 | Pennwalt Corporation | Process for producing polymer bound hindered amine light stabilizers |
-
1992
- 1992-11-24 DE DE4239437A patent/DE4239437A1/de not_active Withdrawn
-
1993
- 1993-11-15 DK DK94900812.2T patent/DK0670851T3/da active
- 1993-11-15 DE DE59305550T patent/DE59305550D1/de not_active Expired - Lifetime
- 1993-11-15 JP JP51270594A patent/JP3199744B2/ja not_active Expired - Lifetime
- 1993-11-15 AT AT94900812T patent/ATE149182T1/de active
- 1993-11-15 EP EP94900812A patent/EP0670851B1/de not_active Expired - Lifetime
- 1993-11-15 KR KR1019950702087A patent/KR100299150B1/ko not_active Expired - Lifetime
- 1993-11-15 WO PCT/EP1993/003202 patent/WO1994012544A1/de not_active Ceased
- 1993-11-15 ES ES94900812T patent/ES2098904T3/es not_active Expired - Lifetime
- 1993-11-15 SK SK670-95A patent/SK67095A3/sk unknown
- 1993-11-18 TW TW082109695A patent/TW314528B/zh not_active IP Right Cessation
- 1993-11-24 CN CN93120327A patent/CN1105731C/zh not_active Expired - Lifetime
-
1997
- 1997-05-09 GR GR970401053T patent/GR3023399T3/el unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE202011000090U1 (de) | 2011-01-14 | 2011-04-21 | E-LEAD ELECTRONIC CO., LTD., Shengang Shiang | Fahrzeug-Audiosystem mit auswechselbarem Plug-In-Computer |
Also Published As
| Publication number | Publication date |
|---|---|
| DE59305550D1 (de) | 1997-04-03 |
| CN1091434A (zh) | 1994-08-31 |
| DE4239437A1 (de) | 1994-05-26 |
| JPH08505648A (ja) | 1996-06-18 |
| WO1994012544A1 (de) | 1994-06-09 |
| DK0670851T3 (zh) | 1997-03-17 |
| ES2098904T3 (es) | 1997-05-01 |
| EP0670851A1 (de) | 1995-09-13 |
| EP0670851B1 (de) | 1997-02-26 |
| GR3023399T3 (en) | 1997-08-29 |
| JP3199744B2 (ja) | 2001-08-20 |
| CN1105731C (zh) | 2003-04-16 |
| KR950704371A (ko) | 1995-11-20 |
| SK67095A3 (en) | 1995-10-11 |
| ATE149182T1 (de) | 1997-03-15 |
| KR100299150B1 (ko) | 2001-10-22 |
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